Netchine I - Search Results

1

IGF2: Development, Genetic and Epigenetic Abnormalities.

Sélénou C, Brioude F, Giabicani E, Sobrier ML, Netchine I. Sélénou C, et al. Among authors: netchine i. Cells. 2022 Jun 10;11(12):1886. doi: 10.3390/cells11121886. Cells. 2022. PMID: 35741015 Free PMC article. Review.

2

Pituitary stalk interruption syndrome: a clinical-biological-genetic assessment of its pathogenesis.

Pinto G, Netchine I, Sobrier ML, Brunelle F, Souberbielle JC, Brauner R. Pinto G, et al. Among authors: netchine i. J Clin Endocrinol Metab. 1997 Oct;82(10):3450-4. doi: 10.1210/jcem.82.10.4295. J Clin Endocrinol Metab. 1997. PMID: 9329385

3

Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency.

Netchine I, Sobrier ML, Krude H, Schnabel D, Maghnie M, Marcos E, Duriez B, Cacheux V, Moers Av, Goossens M, Grüters A, Amselem S. Netchine I, et al. Nat Genet. 2000 Jun;25(2):182-6. doi: 10.1038/76041. Nat Genet. 2000. PMID: 10835633

4

[Molecular pathology of transcription factors implicated in the development of the anterior hypophysis].

Netchine I, Sobrier ML, Amselem S. Netchine I, et al. Arch Pediatr. 2000 May;7 Suppl 2:218s-220s. doi: 10.1016/s0929-693x(00)80044-5. Arch Pediatr. 2000. PMID: 10904717 French. No abstract available.

5

Syndromic short stature in patients with a germline mutation in the LIM homeobox LHX4.

Machinis K, Pantel J, Netchine I, Léger J, Camand OJ, Sobrier ML, Dastot-Le Moal F, Duquesnoy P, Abitbol M, Czernichow P, Amselem S. Machinis K, et al. Among authors: netchine i. Am J Hum Genet. 2001 Nov;69(5):961-8. doi: 10.1086/323764. Epub 2001 Sep 20. Am J Hum Genet. 2001. PMID: 11567216 Free PMC article.

6

Alu-element insertion in the homeodomain of HESX1 and aplasia of the anterior pituitary.

Sobrier ML, Netchine I, Heinrichs C, Thibaud N, Vié-Luton MP, Van Vliet G, Amselem S. Sobrier ML, et al. Among authors: netchine i. Hum Mutat. 2005 May;25(5):503. doi: 10.1002/humu.9332. Hum Mutat. 2005. PMID: 15841484

7

Complex disease phenotype revealed by GH deficiency associated with a novel and unusual defect in the GH-1 gene.

Iughetti L, Sobrier ML, Predieri B, Netchine I, Carani C, Bernasconi S, Balli F, Amselem S. Iughetti L, et al. Among authors: netchine i. Clin Endocrinol (Oxf). 2008 Jul;69(1):170-2. doi: 10.1111/j.1365-2265.2007.03157.x. Epub 2008 Jul 1. Clin Endocrinol (Oxf). 2008. PMID: 18088397 No abstract available.

8

[Epigenetics, genomic imprinting and developmental disorders].

Le Bouc Y, Rossignol S, Azzi S, Brioude F, Cabrol S, Gicquel C, Netchine I. Le Bouc Y, et al. Among authors: netchine i. Bull Acad Natl Med. 2010 Feb;194(2):287-97; discussion 297-300. Bull Acad Natl Med. 2010. PMID: 21166119 French.

9

Imprinted anomalies in fetal and childhood growth disorders: the model of Russell-Silver and Beckwith-Wiedemann syndromes.

Netchine I, Rossignol S, Azzi S, Brioude F, Le Bouc Y. Netchine I, et al. Endocr Dev. 2012;23:60-70. doi: 10.1159/000341750. Epub 2012 Nov 23. Endocr Dev. 2012. PMID: 23182821

10

Epigenetic anomalies in childhood growth disorders.

Netchine I, Rossignol S, Azzi S, Le Bouc Y. Netchine I, et al. Nestle Nutr Inst Workshop Ser. 2013;71:65-73. doi: 10.1159/000342568. Epub 2013 Jan 22. Nestle Nutr Inst Workshop Ser. 2013. PMID: 23502140

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